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Scoliosis clinical trials

View clinical trials related to Scoliosis.

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NCT ID: NCT02084342 Active, not recruiting - Clinical trials for Idiopathic Scoliosis

Study of DDAVP Combined With TXA on the Blood Loss and Transfusion Need During and After Scoliosis Correction Surgery

Start date: December 2013
Phase: N/A
Study type: Interventional

Intraoperative administration of tranexamic acid (TXA,T) reduces significantly blood loss and blood transfusion requirements during spinal posterior fusion in adolescents with scoliosis. TXA acts mainly by inhibit the plasminogen activator. Desmopressin (DDAVP ,D) can inhibit the fibrinolytic activity by inducing the release of von Willebrand factor from the endothelial cells. But at the same time, it releases tissue-type plasminogen activator (t-PA), which may cripple its hemostatic effect. The investigators supposed that if the investigators combine TXA with DDAVP in scoliosis correction surgery, the blood loss and the transfusion need would be reduced significantly.

NCT ID: NCT02084264 Terminated - Scoliosis Clinical Trials

Robotic vs. Freehand Corrective Surgery for Pediatric Scoliosis

PEDSCOLI
Start date: October 2014
Phase:
Study type: Observational

To compare the accuracy and feasibility, curvature correction and clinical outcomes of pedicle screw instrumentation with versus without robotic guidance, in pediatric and adolescent scoliosis patients

NCT ID: NCT02080611 Withdrawn - Scoliosis Clinical Trials

Smart Textile Technology for Scoliosis

Start date: January 2016
Phase: N/A
Study type: Observational

The investigators hypothesize that a garment-integrated sensing system will be able to detect with clinical accuracy the position of the spine. The investigator will evaluate this using healthy adult volunteers, who will don sensing garments and assume a series of spinal postures. Concurrent with garment sensing, the participant's spine position will be measured using a motion-capture system that uses reflective markers to detect positions of markers in 3D space. The motion-capture system provides a gold-standard reference measure to which the sensing garments will be compared. Because the investigators are evaluating the accuracy of the sensing garment, it is only necessary that the investigator test the garments on participants with subtly different body shapes. Healthy adult volunteers provide an adequate input to the sensing signal.

NCT ID: NCT02064101 Completed - Scoliosis Clinical Trials

Validation of Triggered EMG Values for Pedicle Screws Using a Powered Screwdriver

Start date: February 2014
Phase: N/A
Study type: Observational

Previous studies have shown how triggered electromyogram (EMG) pedicle screw stimulation can be used to effectively test correct pedicle screw placement in the lumbar and thoracic vertebrae. Most papers agree that if more than 6mA of current are needed to elicit a response the screw is correctly placed in the bone. If there is a response with less than 6mA there is a strong likelihood of a breach of the pedicle wall or invasion of the spinal canal. Typically this triggered EMG stimulation is done after all the screws have been placed with a ball-tipped probe and is paired with intraoperative fluoroscopy to ensure correct placement of the screws. Another method of testing the current for each screw is with a powered screwdriver, which can stimulate and give a reading as the surgeon places each screw. Both of these methods are currently used by surgeons, however the powered screwdriver has been found to be a faster method. The investigator's aim with this study is to compare these two methods of testing triggered EMG values. The investigators plan on doing this by testing each screw with both the ball-tipped probe and the powered screwdriver, in order to see if there are any statistically significant differences between the readings.

NCT ID: NCT02062606 Terminated - Clinical trials for Adolescent Idiopathic Scoliosis

MESA Railâ„¢ AIS Study - Preservation of Curve Correction

Start date: May 2014
Phase:
Study type: Observational

To evaluate the restoration and maintenance of thoracic kyphosis and coronal curve correction demonstrated through the surgical implantation of the K2M MESA Railâ„¢ Deformity System as compared to literature reported outcomes for standard Cobalt Chrome (CoCr) rod systems in the treatment of Adolescent Idiopathic Scoliosis (AIS).

NCT ID: NCT02058238 Withdrawn - Scoliosis Clinical Trials

ADDRESS - Adult Deformity Robotic vs. Freehand Surgery to Correct Spinal Deformity

Start date: October 3, 2014
Phase:
Study type: Observational

To quantify potential short- and long-term benefits of robotically-guided minimally invasive (MIS) or open-approach spine surgery in adult patients undergoing multi-level spinal instrumentation surgery, in comparison to image- or navigation-guided instrumentation in a matching cohort of control patients, performed using a freehand technique, both in MIS and open approaches.

NCT ID: NCT01900626 Terminated - Clinical trials for Adolescent Idiopathic Scoliosis

Single vs Double Epidural Catheter Analgesia for Scoliosis Surgery

Start date: July 2013
Phase: N/A
Study type: Interventional

This is a study comparing pain control utlilizing one or two epidural catheters, along with a hydromorphone PCA, for analgesia following surgery for correction of scoliosis.

NCT ID: NCT01852747 Terminated - Scoliosis Clinical Trials

Comparison of Actifuse ABX and Local Bone in Spinal Surgery

Start date: March 2013
Phase: Phase 4
Study type: Interventional

This study is being done to compare people who had a standard of care spinal fusion using part of their local bone graft (a small amount of bone from the region of the spine where the fusion is occurring) to correct an adult spinal deformity and people who will have a standard of care spinal fusion using a mixture of Actifuse ABX® (a market approved bone graft substitute) and a local bone graft (a small amount of bone from the region of the spine where the fusion is occurring). This study will compare the outcomes of both groups to help the Orthopaedic surgeon conducting spinal fusions in the future. Investigators expect that Actifuse ABX® will be as good if not better than just a local bone graft.

NCT ID: NCT01820845 Completed - Scoliosis Clinical Trials

Accuracy of Pleth Variability Index (PVI) in Children

PVI
Start date: December 2012
Phase: N/A
Study type: Observational

Plethysmographic Variability index is a simple index accurate in predicting fluid responsiveness. The aim of this study was to investigate its accuracy in predicting fluid response to intravenous fluid challenge during scoliosis surgery in children.

NCT ID: NCT01813058 Completed - Clinical trials for Adolescent Idiopathic Scoliosis

Does Tranexamic Acid Decrease Blood Loss in Pediatric Idiopathic Scoliosis Surgery?

Start date: January 2013
Phase: Phase 1/Phase 2
Study type: Interventional

Adolescent idiopathic scoliosis surgery is an extensive procedure associated with significant blood loss frequently requiring the transfusion of blood. Tranexamic acid (TXA) is a synthetic antifibrinolytic (prevents breakdown of the blood clot) that has been used to extensively reduce transfusion in pediatric major surgery, including cardiac, craniofacial and orthopedic surgery. In this prospective randomized double-blinded study, the investigators wish to evaluate the hypothesis that TXA is more effective than standard of care at decreasing blood loss and blood transfusion perioperatively in children and adolescents undergoing idiopathic scoliosis surgery.